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1

Journal Article

Autoradiographic comparison of in vitro binding characteristics of various tritiated adenosine A2A receptor ligands in rat, mouse and pig brain and first ex vivo results

Sihver, W.
2009

European journal of pharmacology / Environmental toxicology and pharmacology, 616 (2009)

“...MeSH Receptor, Adenosine A2A: metabolism...”

2

Journal Article

Synthesis and evaluation of 7-amino-2(2(3)-furyl)-5-phentylethylaminooxazolo[4,5-d]pyrimidines as potential A2A adenosine receptor antagonist for positron emission tomography (PET)

Holschbach, M. H.
2006

European Journal of Medicinal Chemistry, 41 (2006) S. 7 - 15

“...MeSH Receptor, Adenosine A2A: metabolism...”

3

Journal Article

Derivatives of 4,6-diamino-1,2-dihydro-2-phenyl-1,2,4-triazolo[4,3-alpha]quinoxalin-1-ones as potential antagonist ligands for imaging the A2A receptor by positron emission tomography (PET)

Holschbach, M. H.
2005

European Journal of Medicinal Chemistry, 40 (2005) S. 421 - 437

4

Journal Article

Synthese, Markierung und Evaluierung von 2,6-Diaminopurinen als potentielle A2A-Adenosin-Rezeptorliganden für die PET

Breidenbach, M.
2004

Nuklearmedizin, 43 (2004) S. A114

5

Journal Article

Binding of tritiated and radioiodinated Zm241,385 to brain A2A adenosine receptors

Sihver, W.
2004

Nuclear medicine and biology, 31 (2004) S. 173 - 177

“...MeSH Receptor, Adenosine A2A: metabolism...”

6

Journal Article

Evaluation of radioiodinated 8-cyclopentyl-3-[(E)-3-iodoprop-2-en-1-YL]-1-propylxanthine ([* I]CPIPX) as a new potential A1 adenosine receptor antagonist for SPECT

Sihver, W.
2003

Nuclear medicine and biology, 30 (2003) S. 661 - 668

7

Journal Article

Tritium-labelled 8-cyclopentyl-3-(3-fluoropropyl)-1-propylxanthine ([3H]CPFPX), a potent and selective antagonist for the A1 adenosine receptor

Holschbach, M. H.
2003

Journal of labelled compounds and radiopharmaceuticals, 46 (2003) S. 365 - 372

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